rs1047016803
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1047016803(C;T) |
Make rs1047016803(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 57651502 |
Gene | ADGRG1 |
is a | snp |
is | mentioned by |
dbSNP | rs1047016803 |
dbSNP (classic) | rs1047016803 |
ClinGen | rs1047016803 |
ebi | rs1047016803 |
HLI | rs1047016803 |
Exac | rs1047016803 |
Gnomad | rs1047016803 |
Varsome | rs1047016803 |
LitVar | rs1047016803 |
Map | rs1047016803 |
PheGenI | rs1047016803 |
Biobank | rs1047016803 |
1000 genomes | rs1047016803 |
hgdp | rs1047016803 |
ensembl | rs1047016803 |
geneview | rs1047016803 |
scholar | rs1047016803 |
rs1047016803 | |
pharmgkb | rs1047016803 |
gwascentral | rs1047016803 |
openSNP | rs1047016803 |
23andMe | rs1047016803 |
SNPshot | rs1047016803 |
SNPdbe | rs1047016803 |
MSV3d | rs1047016803 |
GWAS Ctlg | rs1047016803 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1047016803(T;T) |
Alt | rs1047016803(T;T) |
Reference | Rs1047016803(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ADGRG1 GPR56 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.57685414C>T |
CLNSRC | |
CLNACC | RCV000434335.1, |